Since our founding in 1994, QPharma, Inc. has been at the forefront of regulatory compliance for the highly regulated life sciences industries. Today, as the leader in cloud-based software and services for the life sciences industry, QPharma fulfills our role as a trusted partner to our valued clients. Every solution we provide is built on a robust foundation of quality and regulatory compliance, enabling clients to pursue commercial success while adhering to complex guidelines and regulations enforced by FDA, CMS, and other regulatory authorities.
Headquartered in Morristown, New Jersey, with offices planned in Europe, Asia, and Latin America, QPharma commands respect throughout the industry for our commitment to quality and superior service. QPharma’s consultants, project managers, and subject matter experts possesses the extensive knowledge, access to resources, and key regulatory contacts necessary to excel in the execution of any project or engagement — whether working with a brand team to launch and promote a new product, or developing and implementing major remediation activities for a manufacturer under federal consent decree.
Committed to the satisfaction of our clients — and attuned to the needs of the patients, practitioners, and consumers they serve — QPharma works tirelessly to deliver the most exceptional service possible. Regardless of your brand or compliance need, we’ve got you covered.
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